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3-Hydroxy-4-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
$35.01 - $310.25
Chemical Identifiers
| CAS | 621-59-0 |
|---|---|
| Molecular Formula | C8H8O3 |
| Molecular Weight (g/mol) | 152.149 |
| MDL Number | MFCD00003369 |
| InChI Key | JVTZFYYHCGSXJV-UHFFFAOYSA-N |
| Synonym | isovanillin, isovanilline, 3-hydroxy-p-anisaldehyde, 5-formylguaiacol, benzaldehyde, 3-hydroxy-4-methoxy, iso-vanillin, 3-hydroxyanisaldehyde, isovanilin, isovanicaline, 3-hydroxy-4-methoxy-benzaldehyde |
| PubChem CID | 12127 |
| IUPAC Name | 3-hydroxy-4-methoxybenzaldehyde |
| SMILES | COC1=C(C=C(C=C1)C=O)O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1286606
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Thermo Scientific Chemicals
A1286606 |
5 g |
Each for $35.01
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AAA1286614
|
Thermo Scientific Chemicals
A1286614 |
25 g |
Each for $115.63
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AAA1286622
|
Thermo Scientific Chemicals
A1286622 |
100 g |
Each for $310.25
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Description
3-Hydroxy-4-methoxybenzaldehyde acts as a precursor for the stereoselective synthesis of the anticancer drug (Z)-combretastatin A-4 and glycitein. It also used as an important raw material for the preparation of morphine. Further, it is involved in the preparation of Schiff- bases by reacting with furan-2-carboxylic acid hydrazide and thiophene-2-carboxylic acid hydrazide. In addition to this, it is used to prepare (Z)-2-(3-hydroxy-4-methoxybenzylidene)-1-azabicyclo[2.2.2]octan-3-one by reacting with with1-azabicyclo[2.2.2]octan-3-one.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications3-Hydroxy-4-methoxybenzaldehyde acts as a precursor for the stereoselective synthesis of the anticancer drug (Z)-combretastatin A-4 and glycitein. It also used as an important raw material for the preparation of morphine. Further, it is involved in the preparation of Schiff- bases by reacting with furan-2-carboxylic acid hydrazide and thiophene-2-carboxylic acid hydrazide. In addition to this, it is used to prepare (Z)-2-(3-hydroxy-4-methoxybenzylidene)-1-azabicyclo[2.2.2]octan-3-one by reacting with with1-azabicyclo[2.2.2]octan-3-one.
Solubility
Soluble in acetone and methanol.
Notes
Air sensitive. Store in a cool place. Incompatible with strong oxidizing agents and strong bases.
Chemical Identifiers
| 621-59-0 | |
| 152.149 | |
| JVTZFYYHCGSXJV-UHFFFAOYSA-N | |
| 12127 | |
| COC1=C(C=C(C=C1)C=O)O |
| C8H8O3 | |
| MFCD00003369 | |
| isovanillin, isovanilline, 3-hydroxy-p-anisaldehyde, 5-formylguaiacol, benzaldehyde, 3-hydroxy-4-methoxy, iso-vanillin, 3-hydroxyanisaldehyde, isovanilin, isovanicaline, 3-hydroxy-4-methoxy-benzaldehyde | |
| 3-hydroxy-4-methoxybenzaldehyde |
Specifications
| 621-59-0 | |
| 1.2 | |
| >110°C (230°F) | |
| MFCD00003369 | |
| 1073021 | |
| isovanillin, isovanilline, 3-hydroxy-p-anisaldehyde, 5-formylguaiacol, benzaldehyde, 3-hydroxy-4-methoxy, iso-vanillin, 3-hydroxyanisaldehyde, isovanilin, isovanicaline, 3-hydroxy-4-methoxy-benzaldehyde | |
| JVTZFYYHCGSXJV-UHFFFAOYSA-N | |
| 3-hydroxy-4-methoxybenzaldehyde | |
| 12127 | |
| 98% |
| 112°C to 116°C | |
| 179°C (15 mmHg) | |
| C8H8O3 | |
| 5 g | |
| Air and light sensitive | |
| Soluble in acetone and methanol. | |
| COC1=C(C=C(C=C1)C=O)O | |
| 152.149 | |
| 152.15 | |
| 3-Hydroxy-4-methoxybenzaldehyde |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
EINECSNumber : 210-694-9
RTECSNumber : CU6540000
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only